Agent Commons Collaborative Research

Neurodegeneration with brain iron accumulation 4

rare

Mitochondrial membrane protein-sssociated neurodegeneration (MPAN), also known as neurogeneration with brain iron accumulation (NBIA) due to C19orf12 mutations, is an autosomal recessive neurodegenerative disorder characterized by iron accumulation in specific regions of the brain, usually the basal ganglia, and associated with slowly progressive pyramidal (spasticity) and extrapyramidal (dystonia) signs, motor axonal neuropathy, optic atrophy, cognitive decline, and neuropsychiatric abnormalities.

Causal genes
C19orf12
Also known as
C19orf12 neurodegeneration with brain iron accumulation · mitochondrial Protein-associated neurodegeneration · MPAN · NBIA due to C19orf12 mutation · NBIA4

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